Metecon at Swiss Medtech Day 2023

We are pleased that this year we will be exhibiting at the prestigious Swiss Medtech Day, the leading conference for the Swiss medical technology industry. This event offers us a great opportunity to exchange ideas with industry experts, expand our network and establish valuable partnerships.

And that's not all, we have more exciting news for you: Metecon Schweiz GmbH has officially started operations in Bern and is now available to you together with Metecon GmbH with all our proven regulatory compliance services. In addition, we are now also the CH-REP for companies wishing to launch their products in Switzerland. And as a trusted partner in the areas of Technical Documentation, Regulatory Affairs, Clinical Affairs and Quality Management, we will advise and support Swiss medical device companies in navigating through complex regulatory requirements.

We cordially invite you to visit our booth at the Swiss Medtech Day. Come by and learn more about our extensive range of services. Jörg Ohmer, Head of Business Development, and his colleague Oliver Schaer look forward to meeting you in person and discussing your current challenges!
Our blog posts are researched and created with the utmost care, but are only snapshots of the regulations, which are constantly changing. We do not guarantee that older content is still current or meaningful. If you are not sure whether the article you have read on this page still corresponds to the current state of regulation, please contact us: we will quickly place your topic in the current context.

Subscribe to our newsletter and benefit from our expertise

Regulatory compliance requires in-depth and comprehensive knowledge. Our newsletter provides you with both of these: Every 14 days, it provides you with best practices from our experts in documentation, market access and monitoring. It offers information on current events, topic overviews, and tips for implementation – in short: Our newsletter keeps you up to date.

Subscribe to our newsletter and receive our free information service

Try our Quick Help!

Often all it takes is a little help, a nudge in the right direction, to get back on track. That is what our Quick Help is for: you ask, we answer - FREE, fast and easy.

Are you stuck, going in circles with a question about Technical Documentation, QM, Verification, Validation, Clinical Affairs or Regulatory Affairs? What are you waiting for?

Put us to the test!

Regulatory History: Blog Archive

You can find older posts in our blog archive. Please make sure that this content is up to date before using it; we are happy to help.